Evidence map›Paper›PMID 40961784›Full record

ArticleJournal of critical care2026

Evaluation of opioid requirements in mechanically ventilated patients taking buprenorphine/naloxone prior to admission.

Molly O'Connell, Ashley Kamp, Sean Mertz, Michelle Kuhrt, Lexie Zidanyue Yang, Alaattin Erkanli, Christopher E Cox, Bridgette Kram

Abstract readMulticenter Study
In one paragraph

Article in Journal of critical care, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Molly O'ConnellDuke University Hospital, Department of Pharmacy, Durham, NC, United States of America. Electronic address: molly.oconnell@duke.edu.
Ashley KampDuke University Hospital, Department of Pharmacy, Durham, NC, United States of America.
Sean MertzDuke University Hospital, Department of Pharmacy, Durham, NC, United States of America.
Michelle KuhrtDuke University Hospital, Department of Pharmacy, Durham, NC, United States of America.
Lexie Zidanyue YangDuke University School of Medicine, Department of Biostatistics and Bioinformatics, Durham, NC, United States of America.
Alaattin ErkanliDuke University School of Medicine, Department of Biostatistics and Bioinformatics, Durham, NC, United States of America.
Christopher E CoxDepartment of Medicine, Division of Pulmonology, Allergy, and Critical Care, Durham, NC, United States of America.
Bridgette KramDuke University Hospital, Department of Pharmacy, Durham, NC, United States of America.

Funding

Support for QA/QC for Prior Approval ProcessUL1TR002553 · NCATS · DUKE UNIVERSITY · PI LI, JENNIFER S, MCNAMARA, JAMES O. · 2018 to 2023
$58.5M
NCATS NIH HHS UL1 TR002553
6 · The paper itself

Abstract

backgroundWith limited data quantifying opioid requirements based on substance use history, including buprenorphine/naloxone use, optimal pain management for mechanically ventilated patients remains unknown.

objectiveTo compare opioid requirements in mechanically ventilated adults admitted to the intensive care unit (ICU) taking buprenorphine/naloxone prior to admission compared to those who do not.

methodsThis multicenter, retrospective study included adults admitted to a medical ICU and mechanically ventilated for at least 12 h. The primary endpoint was mean hourly opioid rate (fentanyl equivalents [FE], μg FE/h) from intubation until extubation or up to 72 h. Secondary endpoints included sedative requirements and time with pain and depth of sedation scores within goal. To adjust for confounders, a negative binomial model was performed.

resultsOf 176 patients, 47 took buprenorphine/naloxone, 69 were opioid-naïve, and 60 were opioid-tolerant. There was no difference in mean hourly opioid rate between buprenorphine/naloxone (40.8 ± 37.1 μg FE/h) and opioid-naïve (31.7 ± 32.5 μg FE/h; p = 0.17) and opioid-tolerant patients (51 ± 46 μg FE/h; p = 0.22). Multivariable regression demonstrated similar hourly rates in buprenorphine/naloxone and opioid-naïve patients, but opioid-tolerant patients had 50 % higher rates (estimated rate ratio 1.5, 95 % CI [1.01, 2.23]). Time spent with pain scores at goal was similar. Time spent with sedation scores at goal was similar between buprenorphine/naloxone and opioid-naïve patients, but was lower than opioid-tolerant patients.

conclusionPatients taking buprenorphine/naloxone prior to admission who are mechanically ventilated for at least 12 h may have opioid requirements similar to opioid-naïve patients and lower than opioid-tolerant patients.

Indexed as

Analgesics, OpioidBuprenorphineBuprenorphine, Naloxone Drug CombinationNaloxoneNarcotic AntagonistsPain ManagementRespiration, ArtificialAdultAgedFemaleHumansIntensive Care UnitsMaleMiddle AgedRetrospective StudiesAnalgesics, OpioidBuprenorphineBuprenorphine, Naloxone Drug CombinationNaloxoneNarcotic AntagonistsAnalgesiaOpioid use disorderSedation

Identifiers

PMID40961784
PMCPMC12614754

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.